GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.

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Epileptic encephalopathies are severe brain disorders with the epileptic component contributing to the worsening of cognitive and behavioral manifestations. Acquired epileptic aphasia (Landau-Kleffner syndrome, LKS) and continuous spike and waves during slow-wave sleep syndrome (CSWSS) represent rar...

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Bibliographic Details
Main Authors: Lesca, G, Rudolf, G, Bruneau, N, Lozovaya, N, Labalme, A, Boutry-Kryza, N, Salmi, M, Tsintsadze, T, Addis, L, Motte, J, Wright, S, Tsintsadze, V, Michel, A, Doummar, D, Lascelles, K, Strug, L, Waters, P, de Bellescize, J, Vrielynck, P, de Saint Martin, A, Ville, D, Ryvlin, P, Arzimanoglou, A, Hirsch, E, Vincent, A
Format: Journal article
Language:English
Published: 2013

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